LMNA and Hutchinson-Gilford progeria syndrome: The mutations of LMNA gene cause at least eight types of inherited disorders, including muscular, neurogenic, adiposocytopathies and progeria syndromes, such as Emery–Dreifuss muscular dystrophy type 2[11], limb girdle muscular dystrophy type 1B[12], dilated cardiomyopathy type 1A[13], Charcot–Marie–Tooth disease type 2B1[14], Dunnigan-type familial partial lipodystrophy[15], MAD, HGPS and restrictive dermopathy (RD)[16].